Designation: C 637 98a (Reapproved 2003)
Standard Specification for
Aggregates for Radiation-Shielding Concrete1
This standard is issued under the fixed designation C 637; the number immediately following the designation indicates the year of
original adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. A
superscript epsilon (e) indicates an editorial change since the last revision or reapproval.
This standard has been approved for use by agencies of the Department of Defense.
1. Scope
1.1 This specification covers special aggregates for use in
radiation-shielding concretes in which composition or high
specific gravity, or both, are of prime consideration.
1.2 The values stated in SI units are to be regarded as the
standard. The values given in parentheses are for information
only.
1.3 The following precautionary caveat pertains only to the
test method portion, Section 8, of this specification:This
standard does not purport to address all of the safety concerns,
if any, associated with its use. It is the responsibility of the user
of this standard to establish appropriate safety and health
practices and determine the applicability of regulatory limita-
tions prior to use.
2. Referenced Documents
2.1 ASTM Standards: 2
C 33 Specification for Concrete Aggregates
C 127 Test Method for Density, Relative Density (Specific
Gravity) and Absorption of Coarse Aggregate
C 128 Test Method for Density, Relative Density, (Specific
Gravity) and Absorption of Fine Aggregate
C 131 Test Method for Resistance to Degradation of Small-
Size Coarse Aggregate by Abrasion and Impact in the Los
Angeles Machine
C 136 Test Method for Sieve Analysis of Fine and Coarse
Aggregates
C 535 Test Method for Resistance to Degradation of Large-
Size Coarse Aggregate by Abrasion and Impact in the Los
Angeles Machine
C 638 Descriptive Nomenclature of Constituents of Aggre-
gates for Radiation-Shielding Concrete
1
This specification is under the jurisdiction of ASTM Committee C09 on
Concrete and Concrete Aggregates and is the direct responsibility of Subcommittee
C09.41 on Concrete for Radiation Shielding.
Current edition approved May 10, 1998. Published December 1998. Originally
approved in 1969. Last previous edition approved in 1998 as C 637 98a.
2
For referenced ASTM standards, visit the ASTM website, www.astm.org, or
contact ASTM Customer Service at service@astm.org. For Annual Book of ASTM
Standards volume information, refer to the standards Document Summary page on
the ASTM website.
Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.
1
3. Classification
3.1 Aggregates covered by this specification include:
3.1.1 Natural mineral aggregates of either high density or
high fixed water content, or both. These include aggregates that
contain or consist predominately of materials such as barite,
magnetite, hematite, ilmenite, and serpentine.
3.1.2 Synthetic aggregates such as iron, steel, ferrophospho-
rus and boron frit or other boron compounds (see Descriptive
Nomenclature C 638).
3.1.3 Fine aggregate consisting of natural or manufactured
sand including high-density minerals. Coarse aggregate may
consist of crushed ore, crushed stone, or synthetic products, or
combinations or mixtures thereof.
4. Composition and Specific Gravity
4.1 Table 1 gives data on chemical composition and specific
gravity of aggregate materials covered by this specification.
4.2 The purchaser shall specify the minimum specific grav-
ity for each size and type of aggregate.
4.2.1 Uniformity of Specific GravityThe bulk specific
gravity (saturated surface-dry) of successive shipments of
aggregate shall not differ by more than 3 % from that of the
sample submitted for source approval tests. The average
specific gravity of the total shipment shall be equal to or greater
than the specified minimum.
4.3 The purchaser shall specify the minimum fixed water
content of hydrous ores. If the design temperature, T, is
different from that given in 8.1.3.5, the purchaser shall specify
the value of T.
4.3.1 Uniformity of Fixed Water ContentFor hydrous
aggregates the fixed water content of successive shipments of
aggregate shall not be less than 95 % of the specified minimum
value. The average fixed water content of the total shipment
shall be equal to or exceed the specified minimum value.
5. Aggregate Grading
5.1 Sieve AnalysisFine and coarse aggregates for conven-
tionally placed concrete shall be graded within the limits given
in Specification C 33, except that with the approval of the
purchaser, as much as 20 % of the material passing the 9.5-mm
(38 -in.) sieve may also pass the 150-m (No. 100) sieve, with
 C 637 98a (2003)
TABLE 1 Composition and Specilc Gravity of Aggregates Covered by This Speciflcation
Specific Gravity of
Predominant Chemical Composition of
Class of Material Available
Constituent Principal ConstituentA
Aggregates
SerpentineB crushed stone, hydrous siliente Mg3Si2O5(OH)4 2.4 to 2.65
LimoniteC crushed stone, hydrous iron ore (HFeO2)x(H2O)y 3.4 to 3.8
GoethiteC crushed stone, hydrous iron ore HFeO2 3.5 to 4.5
Barite gravel or crushed stone BaSO4 4.0 to 4.4
Ilmenite crushed stone, iron ore FeTiO3 4.2 to 4.8
Hematite crushed stone, iron ore Fe2O3 4.6 to 5.2
Magnetite crushed stone, iron ore FeFe2O4 4.6 to 5.2
Iron manufactured from iron/steel Fe 6.5 to 7.5
FerrophosphorousD synthetic FenP 5.8 to 6.3
Boron FritE synthetic B2O3, Al2O3, SiO2, CaO 2.6 to 2.8
Boron Carbide synthetic B4C, B2O3, C 2.5
Calcium Boride synthetic CaB6, C 2.5
A
When it is necessary to minimize the production of long-lived secondary radiation in the shield, or to avoid using materials having inherent radioactivity, the purchaser
should specify limits on the contents of objectionable elements.
B
The fixed water content of serpentine ranges from 10 to 13 percent by weight.
C
The fixed water content of limonite and goethite ranges from 8 to 12 percent by weight.
D
Ferrophosphorus when used in Portland cement concrete will generate flammable and possibly toxic gases which can develop high pressures if confined. See
Clendenning, T. G., Kellam, B., and MacInnis, C., Hydrogen Evolution from Ferrophosphorous Aggregate in Portland Cement Concrete, Journal of the American Concrete
Institute, No. 12, December 1968. (Proceedings, Vol 65, pp. 10211028), and Mather, Bryant, discussion of Davis, Harold S., Concrete for Radiation ShieldingIn
Perspective, and closure by author in Concrete for Nuclear Reactors, Journal of the American Concrete Institute SP-34, Vol 1, 1972, pp. 1113.
E
The fixed water content of boron frit is less than 0.5 %.

up to 10 % passing the 75-m (No. 200) sieve if the material 5.2 Fineness ModulusIf the fineness modulus of the fine
passing the 75-m (No. 200) sieve is essentially free of clay or aggregate varies more than 0.2 from the value corresponding to
shale. that of the sample submitted for acceptance, the fine aggregate
5.1.1 Fine and coarse aggregates for preplaced aggregate shall be rejected unless suitable adjustments are made in
concrete shall be graded according to the requirements of Table concrete proportions to compensate for the difference in
2 and as follows: grading.
6. Deleterious Substances
Grading of Aggregate
Specific Gravity Coarse Fine 6.1 Fine and coarse aggregates shall meet the requirements
of Fine Aggregate Aggregate Aggregate of Specification C 33.
Up to 3.0 Grading 1 Grading 1
Greater than 3.0 Grading 1 Grading 2
6.2 Boron frit shall not contain more than 2.0 % of water
Full range Grading 2 Grading 2 soluble material.
NOTE 1This limit is based on concrete mixtures containing no more
5.1.2 When boron frit is used as part of the fine aggregate, than 300 kg/m3(500 lb/yd3) of boron frit.
the grading shall be such that 100 % passes the 4.75-mm (No.
4) sieve and not more than 5 % passes the 600-m (No. 30) 7. Abrasion Resistance of Coarse Aggregate
sieve. 7.1 Coarse aggregate shall have an abrasion loss not greater
than 50 % when tested in accordance with Test Method C 131,
TABLE 2 Grading Requirements for Coarse and Fine Aggregates or Test Method C 535, as applicable. Coarse aggregate failing
for Preplaced Aggregate Concrete to meet this requirement may be used, provided it can be
Percentage Passing shown that it produces satisfactory strengths in concrete of the
Grading 1
Grading 2 proportions selected for the work.
Sieve Size For 25-mm (1-in.) Nominal
For 37.5-mm (112 -in.)
Nominal Maximum Size Aggregate
Maximum Size 8. Methods of Sampling and Testing
Aggregate
8.1 Sample and test the aggregates in accordance with the
Coarse Aggregate
methods cited in Specification C 33 as applicable, except as
50-mm (2-in.) 100 ... follows:
37.5-mm (112 in.) 95 to 100 100
25.0-mm (1-in.) 40 to 80 95 to 100 8.1.1 Specific GravityDetermine the bulk specific gravity
19.0-mm (34 in.) 20 to 45 40 to 80 (saturated surface-dry basis) of fine aggregate in accordance
12.5-mm (12-in.) 0 to 10 0 to 15 with Test Method C 128, and of coarse aggregate in accordance
9.5-mm (38-in.) 0 to 2 0 to 2
with Test Method C 127, except that the weight of the test
Fine Aggregate
sample for fine and coarse aggregate shall be approximately the
2.36-mm (No. 8) 100 ... specified weight multiplied by the ratio:
1.18-mm (No. 16) 95 to 100 100
600-m (No. 30) 55 to 80 75 to 95 specific gravity of aggregate/2.65
300-m (No. 50) 30 to 55 45 to 65
150-m (No. 100) 10 to 30 20 to 40 using for specific gravity the higher value given in Table 1.
75-m (No. 200) 0 to 10 0 to 10 8.1.2 Grading Method C 136, except that the weight of
Fineness modulus 1.30 to 2.10 1.00 to 1.60 the test sample for fine and coarse aggregate shall be approxi-
mately the specified weight multiplied by the ratio:

2
 C 637 98a (2003)
specific gravity of aggregate/2.65
using for specific gravity the higher value given in Table 1.
8.1.3 Fixed Water ContentWhen 90 % or more of the
weight loss on ignition of the aggregate is due to fixed water
content, determine the fixed water content, F, by the loss-on-
ignition test according to 8.1.3.1. When less than 90 % of the
loss on ignition is due to fixed water content, determine the
fixed water content by the train method (8.1.3.2). In case of
dispute, use results obtained by the train method as the basis
for acceptance or rejection of the aggregate. Use the train
method to demonstrate that 90 % or more of the weight lost
during ignition is fixed water. When loss-on-ignition tests are
being made on aggregate samples from the same source, also
determine the fixed water content of the first sample and each
tenth sample thereafter by the train method.
8.1.3.1 For the loss-on-ignition test crush a representative
sample of aggregate weighing 20 to 50 g (W) to pass the
4.75-mm (No. 4) sieve. Heat the sample to constant weight at
a temperature, T, in a furnace, open to the atmosphere. Cool the
heated sample in a desiccator and then weigh it, (Wt). Place the
sample in the oven again, heat at the ignition temperature, t,
cool in a desiccator, and determine the final weight (Wt).
Constant weight may be considered to have been attained when
further heating at the design temperature T causes or would
cause less than 0.1 % additional weight loss.
8.1.3.2 In the train test, heat approximately 1 g (W8) of the
finely ground sample to constant weight (W8T) at a temperature
of T. Then heat the sample W8T in a stream of argon gas at the
ignition temperature t. Pass water vapor and gaseous material
driven from the heated sample through magnesium perchlorate.
The gain in weight (W8g) of the magnesium perchlorate is an
indication of the fixed water content of the sample at tempera-
ture T. Also determine the dehydrated weight (W8t) of the
sample at the ignition temperature t.
8.1.3.3 Compute the fixed water content at temperature T by
one of the following equations:
Ignition Test:
F, percent5@~WT2Wt!/WT#3100 (1)
where:
WT = sample heated to constant weight, g, and
Wt = heated and cooled sample, g.
Train Test:
F, percent5@~W8g2W8T!3100 (2)
where:
W8g = gain in weight of sample, g, and
W8T = dehydrated weight, g.
8.1.3.4 Determine the percent of nonhydrous volatile mate-
rial, V, as follows:
Train Test:
V, percent5$@W82~W8t1W8g!#/W8T%3100 (3)
where:
W8 = sample weight, g,
3
W8t = dehydrated weight of sample, g,
W8g = gain in weight of sample, g, and
W8T = sample heated to constant weight, g.
8.1.3.5 Water vapor driven from the sample by heating at
temperature T is considered as part of the nonhydrous volatile
material. Absorbed water at 110C is not considered as part of
the nonhydrous volatile material. Determine percent absorption
by Test Methods C 127 and C 128.
8.1.3.6 Temperature values shall be as follows:
Design Ignition
Temperature, T Temperature, t
Hydrous Aggregate F C F C
Iron ore 230 110 932 500
Serpentine 572 300 1652 900
Heat the sample until it reaches constant weight at the
specified temperature, unless otherwise approved. Determine
weights after sample has been cooled in a desiccator to room
temperature. Duplicate determinations of fixed water content
should check to within 0.3 %.
8.1.4 Water-Soluble Material in Boron FritPlace a 5.00-g
sample passing a 600-m (No. 30) sieve and retained on a
300-m (No. 50) sieve in contact with 100 mL of distilled
water at 20 6 5C for 16 h. Filter, wash with about 200-mL of
hot (70 6 5C) water, and dry at 125 6 10C for 1 h. Weigh
the residue, s, to the nearest 0.01 g. Calculate the percentage of
water soluble material (Ws) to the nearest 0.1 % as follows:
W35@~5.002s!/s]3100
where:
s = residue, g
9. Precision and Bias
9.1 Precision The following precision statement ad-
dresses the test of the water-soluble material in Boron Frit. The
precision for fixed water content by either the loss on ignition
test or by the train test method has not been evaluated.
9.1.1 Data from one laboratory was available for estimating
the precision of water-soluble material in boron frit, therefore,
only a within-laboratory estimate of precision is made. The
estimate is based on 15 replicate analyses of 5 lots of frit
produced by one company. The 15 replicates were determined
on 5 separate days, 3 replicates per day. The mean water
soluble material ranged from 1.23 to 1.75 % among the 5 lots.
9.1.2 Within-laboratory PrecisionThe within-laboratory
standard deviation among individual determinations of water-
soluble material in boron frit is 0.224 %.3 Therefore, two
analyses of the same material should differ by no more than
0.627 %3 in 95 % of cases.
9.2 BiasSince there is no accepted reference material
suitable for determining the bias of this test method, no
statement on bias is made.
3
These numbers represent, respectively, the 1s and d2s limits as described in
Practice C 670.
 C 637 98a (2003)
10. Keywords gates; radiation shielding concrete
10.1 aggregates; boron frit; calcium boride; high-density
aggregates; high water-content aggregates; hydrous aggre-

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